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. Author manuscript; available in PMC: 2013 Feb 1.
Published in final edited form as: J Immunol. 2012 Jan 4;188(3):957–967. doi: 10.4049/jimmunol.1100461

Figure 7. A schematic model summarizing the differential role of SP-A in modulating T cell activation and proliferation depending upon the strength of activating signal.

Figure 7

SP-A allows for low grade, basal levels of proliferation in part by maintaining [Ca2+]i levels, and thus may help maintain the immune repertoire in T cells. Initial expansion in response to strong signals does occur in the presence of SP-A, but it acts as a brake to prevent runaway inflammation at later stages of strong T cell responses. Since extensive proliferation and differentiation to terminal effector cells that ultimately undergo activation induced cell death is avoided, the generation of multifunctional T cells that eventually form memory cells might be enhanced in the presence of SP-A.